Variant report
Variant | rs62461681 |
---|---|
Chromosome Location | chr7:79598767-79598768 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10229737 | 0.92[ASN][1000 genomes] |
rs10237226 | 0.85[EUR][1000 genomes] |
rs12666674 | 1.00[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12667856 | 1.00[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12670640 | 0.85[EUR][1000 genomes] |
rs12670674 | 1.00[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs17153199 | 0.85[EUR][1000 genomes] |
rs1859196 | 0.94[ASN][1000 genomes] |
rs4574785 | 0.85[EUR][1000 genomes] |
rs56191620 | 0.85[EUR][1000 genomes] |
rs62459946 | 1.00[AMR][1000 genomes] |
rs62460731 | 1.00[AMR][1000 genomes] |
rs62461676 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62461679 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62461680 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62461682 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62461685 | 0.85[EUR][1000 genomes] |
rs6946466 | 0.95[ASN][1000 genomes] |
rs757191 | 0.94[ASN][1000 genomes] |
rs981490 | 0.92[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv888522 | chr7:79402551-79619012 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv1032480 | chr7:79558011-79625086 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv429785 | chr7:79589749-80177049 | Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:79597800-79598800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |